A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413803



Internal ID22471673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165039500..165039821hg38UCSC Ensembl
chr4:165960652..165960973hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5903884
Supporting Variants
Samples
Known GenesTRIM60
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413803
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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